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How To Transform Adjacent Complex Variants In Vcf Format To Individuals' Sequences From 1000Genomes Project?

Hello, everyone. Recently, I have downloaded the latest variant data of 1000genomes project from ftp://ftp.ncbi.nlm.nih.gov/1000genomes/ftp/release/20110521/ and the mapped data from ftp://ftp.ncbi.nlm.nih.gov/1000genomes/ftp/data/HG00096/. I want to transform these variants(INDEL and SV) to sequences for each individual. I haven't found any program available to do the job. Therefore, I writed a script according to these rules: 1) For an insert, next_pos=current_pos+1; 2) For a delete or SV, next_pos=current_pos+length(ref_allele). But I encountered some problem for adjacent variants as follows:

CHROM    POS    ID    REF    ALT    HG00096
20    131503    .    ATC    A    1|0:0.940:0.00,-0.70,-31.60
20    131505    rs3079754    CTCT    C    1|0:1.000:-3.20,0.00,-40.50

I got the reference sequence as ATCTCTTG ##chr20:131503-131010. But when I resolved the first position 131503 which resulted the next position as 131506(131503+3) skipping the variant rs3079754, thus I got the sequence A(131503-131505) + TCTTG(131506-131510) as ATCTTG containing the variants. And I observed the mapped result as ATCTG using IGV. Two are different, Which I should choose? Besides, other instances:

20    179735    rs76051089    TTAAAA    T
20    179741    .    TAAAAG    T

The refernce sequence is TTAAAATAAAAGTGAA ##chr20:179735-179750, I got the variant sequence T(179735-179740) + T(179741-179746) + TGAA(179747-179750) as TTTGAA. And the mapped result is TTAAAAAA observed from IGV. Two are different.

20    144831    .    T    TC
20    144832    rs35137860    C    CT

The refernce sequence is TCTTG ##chr20:144831-144835, I got the variant sequence TC(144831) + CT(144832) + TTG(144833-144835) as TCCTTTG. And the mapped result is TCTTTG observed from IGV. Two are different.

20    356672    rs60652239    A    AAAC
20    356674    .    A    AC

The refernce sequence is AAAAA ##chr20:356672-356676, I got the variant sequence AAAC(356672) + A(356673) + AC(356674) + AA(356675-356676)as AAACAACAA. And the mapped result is AAACAACAA observed from IGV. Two are the same.

20    386575    .    GTTCT    G
20    386582    .    CTTTCT    C
20    386585    rs59090432    TC    T

The refernce sequence is GTTCTTTCTTTCTT ##chr20:386575-386588, I got the variant sequence G(386575-386579) + TT(386580-386581) + C(386582-386587) + T(386588) as GTTCT (skipped rs59090432 variant). And the mapped result is GTTCTTTTTT observed from IGV. Two are different.

How do these differences happen, do they originate from MaCH/Thunder imputation? Did I do wrongly? Now I handled variants one by one, should I consider adjacent variants as a whole which is definitely more complex? Or is there any existing program I missed to do the transformation job?

Any suggestions and discussions are welcome. Thanks!

vcf genome indel sv variant
• 3,866 views • link
updated by Gustavo Gustavo • written by Shinvkuo Shinvkuo

Many steps are assuming site independencies. The confliction is a result of that. Just do whatever you like. The VCF is probably wrong. You cannot fix that without going back to the alignment.

• 0 views • link
written by lh3 lh3

1 answer

"But when I resolved the first position 131503 which resulted the next position as 131506(131503+3) skipping the variant rs3079754 [...]"

The coordinates of the variants are relative to the reference. Resolving one variant should not cause a skip of other variants. You might want to process them in reverse numerical order to make it easier.

Looking at your examples:

20 131503 ATC->A & 131505 CTCT->C: I read this as "lose the TC after the A, and lose the TCT after the C", which yields ATCTCTTG -> A(tc)(tct)TG -> ATG... which is different from both results you mentioned...

20 179735 TTAAAA->T & 179741 TAAAAG->T: TTAAAATAAAAGTGAA -> T(taaaa)T(aaaag)TGAA -> TTTGAA = your answer.

20 144831 T->TC & 144832 C->CT: TCTTG -> T(+c)C(+t)TTG -> TCCTTTG = your answer.

20 356672 A->AAAC & 356674 A->AC: AAAAA -> A(+aac)AA(+c)AA -> AAACAACAA = we all agree!

20 386575 GTTCT->G & 386582 CTTTCT->C & 386585 TC->T: GTTCTTTCTTTCTT -> G(ttct)TTC(ttt(c)t)T -> GTTCT = your answer, but UGH, these last two variants DO appear to conflict. My guess is that the former is the "correct" variant and the latter is there simply because it's a previously named variant. Do note these variants are located in the poly-A tail of an AluSx repeat... so there may be mapping issues confounding this spot.

• 1 views • link
written by Gustavo Gustavo

Gustavo, thanks for your reply! I have emailed this problem to 1000genomes group. These two adjacent events could be actually just one. "20 131503 . ATC A" could not exist. If we just discard it (131503), the resolved alt sequence AT(131503-131504, no variant at 131503) + C(131505-131508) + TG(131509-131510) as ATCTG will be the same as the mapped result using IGV.

• 0 views • link
written by Shinvkuo Shinvkuo

Certainly, there still be some events different from the mapped results. I think this problem could be due to sequence self-similarity (like: TCTC[131504-131507], TAAAATAAAA[179736-179745]) around certain regions. And the 1000genomes analysis group may solve it later.

• 0 views • link
written by Shinvkuo Shinvkuo

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